KEGG   VARIANT: 9488v1
Entry
9488v1                      Variant                                
Name
PIGB deficiency
Type
Loss of function
Gene
PIGB  phosphatidylinositol glycan anchor biosynthesis class B [KO:K05286]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 604122
Network
nt06018  GPI-anchor biosynthesis
Disease
H01489  Inherited glycosylphosphatidylinositol deficiencies
Reference
  Authors
Murakami Y, Nguyen TTM, Baratang N, Raju PK, Knaus A, Ellard S, Jones G, Lace B, Rousseau J, Ajeawung NF, Kamei A, Minase G, Akasaka M, Araya N, Koshimizu E, van den Ende J, Erger F, Altmuller J, Krumina Z, Strautmanis J, Inashkina I, Stavusis J, El-Gharbawy A, Sebastian J, Puri RD, Kulshrestha S, Verma IC, Maier EM, Haack TB, Israni A, Baptista J, Gunning A, Rosenfeld JA, Liu P, Joosten M, Rocha ME, Hashem MO, Aldhalaan HM, Alkuraya FS, Miyatake S, Matsumoto N, Krawitz PM, Rossignol E, Kinoshita T, Campeau PM
  Title
Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe Cases.
  Journal
Am J Hum Genet 105:384-394 (2019)
DOI:10.1016/j.ajhg.2019.05.019
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